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A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data

Single-cell RNA sequencing (scRNA-seq) experiments provide opportunities to peer into complex tissues at single-cell resolution. However, insightful biological interpretation of scRNA-seq data relies upon precise identification of cell types. The ability to identify the origin of a cell quickly and...

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Autores principales: Nouri, Nima, Gaglia, Giorgio, Kurlovs, Andre H., de Rinaldis, Emanuele, Savova, Virginia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326446/
https://www.ncbi.nlm.nih.gov/pubmed/37424758
http://dx.doi.org/10.1016/j.mex.2023.102196
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author Nouri, Nima
Gaglia, Giorgio
Kurlovs, Andre H.
de Rinaldis, Emanuele
Savova, Virginia
author_facet Nouri, Nima
Gaglia, Giorgio
Kurlovs, Andre H.
de Rinaldis, Emanuele
Savova, Virginia
author_sort Nouri, Nima
collection PubMed
description Single-cell RNA sequencing (scRNA-seq) experiments provide opportunities to peer into complex tissues at single-cell resolution. However, insightful biological interpretation of scRNA-seq data relies upon precise identification of cell types. The ability to identify the origin of a cell quickly and accurately will greatly improve downstream analyses. We present Sargent, a transformation-free, cluster-free, single-cell annotation algorithm for rapidly identifying the cell types of origin based on cell type-specific markers. We demonstrate Sargent's high accuracy by annotating simulated datasets. Further, we compare Sargent performance against expert-annotated scRNA-seq data from human organs including PBMC, heart, kidney, and lung. We demonstrate that Sargent retains both the flexibility and biological interpretability of cluster-based manual annotation. Additionally, the automation eliminates the labor intensive and potentially biased user annotation, producing robust, reproducible, and scalable outputs. • Sargent is a transformation-free, cluster-free, single-cell annotation algorithm for rapidly identifying the cell types of origin based on cell type-specific markers. • Sargent retains both the flexibility and biological interpretability of cluster-based manual annotation. • Automation eliminates the labor intensive and potentially biased user annotation, producing robust, reproducible, and scalable outputs.
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spelling pubmed-103264462023-07-08 A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data Nouri, Nima Gaglia, Giorgio Kurlovs, Andre H. de Rinaldis, Emanuele Savova, Virginia MethodsX Bioinformatics Single-cell RNA sequencing (scRNA-seq) experiments provide opportunities to peer into complex tissues at single-cell resolution. However, insightful biological interpretation of scRNA-seq data relies upon precise identification of cell types. The ability to identify the origin of a cell quickly and accurately will greatly improve downstream analyses. We present Sargent, a transformation-free, cluster-free, single-cell annotation algorithm for rapidly identifying the cell types of origin based on cell type-specific markers. We demonstrate Sargent's high accuracy by annotating simulated datasets. Further, we compare Sargent performance against expert-annotated scRNA-seq data from human organs including PBMC, heart, kidney, and lung. We demonstrate that Sargent retains both the flexibility and biological interpretability of cluster-based manual annotation. Additionally, the automation eliminates the labor intensive and potentially biased user annotation, producing robust, reproducible, and scalable outputs. • Sargent is a transformation-free, cluster-free, single-cell annotation algorithm for rapidly identifying the cell types of origin based on cell type-specific markers. • Sargent retains both the flexibility and biological interpretability of cluster-based manual annotation. • Automation eliminates the labor intensive and potentially biased user annotation, producing robust, reproducible, and scalable outputs. Elsevier 2023-04-25 /pmc/articles/PMC10326446/ /pubmed/37424758 http://dx.doi.org/10.1016/j.mex.2023.102196 Text en © 2023 Published by Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Bioinformatics
Nouri, Nima
Gaglia, Giorgio
Kurlovs, Andre H.
de Rinaldis, Emanuele
Savova, Virginia
A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data
title A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data
title_full A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data
title_fullStr A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data
title_full_unstemmed A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data
title_short A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data
title_sort marker gene-based method for identifying the cell-type of origin from single-cell rna sequencing data
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326446/
https://www.ncbi.nlm.nih.gov/pubmed/37424758
http://dx.doi.org/10.1016/j.mex.2023.102196
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